Coronary artery bypass surgery was first described 50 years ago (see Chapter 1). During this pioneering era, there were few discussions on which graft to use, with SVGs used exclusively for the first 20 years. Today, all cardiac surgeons are daily face the difficult choice of which graft to use for a selected patient. The choice of conduits depends on several factors, such as the patient’s intrinsic characteristics (age, body mass index, diabetes, pulmonary function, peripheral vascular disease, saphenous vein quality) and extrinsic characteristics (elective or urgent). Additionally, the characteristics of the coronary lesion, including the degree of stenosis, the minimum lumen diameter (MLD), and the fractional flow reserve (FFR) impact the choice of conduits. Even after the graft choice has been made, the manner of using it is still controversial. Some researchers propose in situ graft use, while others prefer free grafts use. When used free, the choice must be made to reimplant the graft in the aorta or in another graft in a composite fashion. The composite assembly is also debated: is it preferable to use a T or a Y shape, and where do we perform this crucial anastomosis? When used in situ, there is no evidence that it is better to use the right internal thoracic artery (ITA) on the left anterior descending (LAD) artery crossing the midline or through the transverse sinus to a first marginal. Moreover, some researchers suggest using one graft per distal anastomosis, while others prefer sequential anastomosis. After patient characteristics, the most important consideration is the coronary lesion itself. Most of the surgical literature on graft patency is based on visual inspection for coronary lesion evaluation. Cardiologists have tried to find a more accurate method to evaluate the severity of the coronary lesion (quantitative coronary angiography (QCA), FFR); unfortunately, these solutions have not been applied to the evaluation of graft performance. Historically, graft patency evaluation has been performed to evaluate the SVG. Since arterial conduits display a totally different endothelial response to shear stress and competitive flow, these historical definitions have become obsolete, leading to new concepts such as “graft functioning.” Moreover, in contradiction to the evidence-based medical literature, there are few evidence-based cardiac surgery reports. Indeed, most of the graft patency literature is retrospective, with few systematic angiographic controls. Most control studies were symptom-driven, leading to a false evaluation of the conduit performance. Recent studies have promoted the use of less-invasive graft evaluations but without evidence of a good correlation with gold-standard angiography. In addition to all discussions regarding graft choice, there is one last powerful factor: “The Surgeon.” Each cardiac surgeon with a given mentorship background is more prone to use a certain graft type even if there is evidence for better performance of another graft. The best example of this phenomenon is the rate of bilateral ITA (BITA) grafting in the USA: 5%, whereas some American surgeons have dedicated their careers to convincing their colleagues that two ITAs are better then one. On the other hand, some European surgeons use BITA in all ages (> 80 years) and without careful evaluation of the coronary lesion. Due to the lack of a clear answer to the question of which graft to use in a specific patient, we decided to investigate the different grafts we used daily: right and left ITA (RITA and LITA, respectively), SVG, and also the right gastroepiploic artery (RGEA). For this purpose, we started 2 prospective randomized trials in 2003 with systematic 6 months functional evaluation. We also performed systematic 6 months and 3 years angiographic evaluation. In the first trial, we studied the various BITA configurations possible to revascularize the left coronary system (Annex 1). In the second, we compared the RGEA versus SVG to revascularize the right coronary artery (RCA) (Annex 2). In addition to these 2 majors trials we analyzed a subgroup of patients with composite Y arterial or venous graft configuration. We used for the first time in literature the FFR in bypass graft to assess the efficiency of this type of assembling (Annex 3-4). We also compared the vasomotion of the free RITA reimplanted in the in-situ LITA with a specific endothelial vasodilatator (Substance P) (Annex 5). Afterwards we analyzed the causes of non-functioning of the free RITA (Annex 6). During the same period, we realized the same analysis with the in-situ LITA and RITA graft (Annex 7). Finally, we analyzed more carefully the coronary lesion with the QCA in order to identify if there was a correlation between the lesion and the graft patency and evaluated a new method to redefine graft patency in relation to the arterial grafting (Annex 2-8-9).
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